HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547721Generated: October 28, 2026
2-Vinylpyridine → HCID 67199350, compound
https://huagongshe.com/reaction/547721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Vinylpyridine | HCID 7521 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 3-Bromo-1-phenyl-5-(pyridin-2-yl)-1,2-dihydropyridin-2-one | HCID 22319065 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67199350 | HCID 67199350 | 8.1% |
Reaction Steps
23 mg of 3-bromo-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-one was dissolved in 20 ml of acetonitrile. To the mixture were added 0.2 mg of palladium acetate, 4.3 mg of tri-o-tolylphosphine and 0.04 ml of triethylamine, followed by stirring at 110° C. in nitrogen atmosphere overnight. To the mixture was added 9.2 mg of 2-vinylpyridine, followed by stirring at 110° C. in nitrogen atmosphere for 5 hours. After cooling to room temperature, the reaction mixture was poured into water, followed by extracting with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel chromatography (hexane/ethyl acetate system), to give 2 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07939549B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-4408c712c04f49c2af114f3346d854ff |
|---|
| Source note | uspto-grants-2011_05 |
|---|